Patient consent to research not always necessary, bioethicists say. ScienceDaily. Retrieved June 2, 2025 from www.sciencedaily.com / releases / 2014 / 02 / 140219173142.htm.

Conclusion. Although consent policies are always evolving, the rationales that underlie the existing consent norms should not be ignored. We need to be sure that the hype and social controversies that ...

This article was originally on a blog post platform and may be missing photos, graphics or links. See About archive blog posts. Participation in clinical trials is critical to progress in medicine ...

Research without consent. Informed consent is rooted in the Nuremberg code of 1947, drafted in the wake of Nazi experimentation. Exception-from-consent studies are rare; ...

Research nurses are well placed to take control of informed consent during a clinical trial. This article discusses research nurses experience of this process during the coronavirus pandemic and how ...

Purpose: To determine the sociodemographic factors associated with consent for storage of DNA for future genetic research. Methods: Analysis of the characteristics of consenting individuals ...

The University IRB applies all Department of Health and Human Services (DHHS) requirements for informed consent to greater than minimal risk research: DHHS general requirements (at 45 CFR 46.116) (see ...

For research involving biospecimens, whether the research will (if known) or might include whole genome sequencing (i.e., sequencing of a human germline or somatic specimen with the intent to generate ...

Although exempt research is exempt from some of the federal regulations, in most cases of interaction with participants, a consent process is indicated. It’s important to understand that even though ...

Version R04 of the Consent Template is now available in the Click Library under the “Templates” tab. Beginning July 1, 2022, the UB IRB will require all new study submissions in Click to use the ...